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Afamelanotide is approved for erythropoietic protoporphyria, a rare genetic condition causing severe phototoxic pain on light exposure. For those patients it is genuinely valuable. It is administered as a controlled-release implant placed by a trained clinician, under a monitoring programme that includes regular skin examination.
A vial from a supplier list is a different product, made to a different standard, without the implant delivery, without the monitoring, and for a different purpose. The approval does not transfer.
Melanotan-1 is more selective for MC1R, which is the pigmentation receptor, so it produces less of the nausea and sexual effects associated with Melanotan-2. That is a real difference and it is the honest argument in its favour.
Systemic melanocyte stimulation acts on all melanocytes, including atypical ones. The monitoring built into the approved programme exists for a reason. Anyone using this outside that programme should have a dermatologist doing regular skin checks and should tell them what they are taking. See Melanotan-2.
Full library · Safety and sourcing · Reconstitution calculator · The 2026 regulatory picture
Regulatory status current as of the page date. This area is changing quickly and this page is reviewed monthly.